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1 o stability of leukocytes labeled with 99mTc-exametazime.
2 with the nonstabilized preparation of 99mTc-exametazime.
3 of leukocytes labeled with stabilized 99mTc-exametazime.
4 LE associated with fresher stabilized 99mTc-exametazime.
5 te labeling with a more stable form of 99mTc-exametazime.
6 orted with the standard preparation of 99mTc-exametazime.
7 ffective preparation of the stabilized 99mTc-exametazime and an extended window for clinical usage, w
8 ar to in vitro results with stabilized 99mTc-exametazime and better than previously reported in vivo
9 ppearance of the mixture of stabilized 99mTc-exametazime and blood components, which makes it impossi
10 concluded that with a small volume of 99mTc-exametazime and double dilution steps with 12.6% ACD/NS
11 6-hr postreconstitution) of stabilized 99mTc-exametazime (approximately 925 MBq, approximately 25 mCi
12 leukocytes labeled with nonstabilized 99mTc-exametazime, (b) leukocytes labeled with stabilized 99mT
13 with 12.6% ACD/NS solution, stabilized 99mTc-exametazime can be used effectively for leukocyte radiol
14 (b) leukocytes labeled with stabilized 99mTc-exametazime containing 250 microg methylene blue, and (c
17 er mixture), the in vitro stability of 99mTc-exametazime has been increased to 4-6 hr postreconstitut
21 lunteers were injected with stabilized 99mTc-exametazime-labeled autologous leukocytes to study label
23 A normal value study of stabilized 99mTc-exametazime-labeled leukocytes has been performed, inclu
26 methylpropylene amine oxide (99mTc-HMPAO, or exametazime) or 99mTc-ethylene-dicysteine diethylester (
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